Statistical SAS Programmer II - Real World Evidence (Portugal home based)
IQVIA
Lisbon, Portugal
há 4 dias

IQVIA Real World Solutions (RWS) Statistical SAS Programmer careers. Exciting new solution-driven jobs based at home (or possibly office based)

We’re hiring Statistical Programmers with great SAS programming skills to join our dynamic Statistical Programming team in Europe & Africa

Why you’ll love working with us :

  • Our careers have a greater purpose - alongside a group of diverse, talented colleagues we work daily on making a real positive impact on human lives and overcoming some of the biggest challenges facing global public health
  • We offer opportunities to work with the leading international healthcare organizations and the latest healthcare trends
  • These are exciting new solution-driven roles as RWS expands into developing further innovations for clients
  • You can progress and shape your long-term career in the direction you choose. With access to industry-leading data and experts, you'll find endless opportunities for growth
  • We offer a competitive salary along with other employee focused benefits for health and recreation, remote working and flexible hours
  • Please only apply if you match the candidate criteria below

    Applications must be in English to be considered

    Your daily missions would include :

  • An RWS SAS Programmer provides statistical programming and data harmonization (for primary and secondary data from multiple sources - EMRs, PROs, eCRF, Observational studies, etc.
  • support & expertise. They advise on database design, data collection and programme tables, listings and figures using SAS (Base SAS, SAS / STAT and SAS Macro) and other applications

  • Conduct statistical analyses for client reports and publications
  • Develop, implement and validate new process technologies, macros and applications under supervision
  • Utilise innovative insights for solution, operations and product development
  • Work directly with both external and internal clients
  • Perform programming quality control checks for source data and report issues
  • Review, detect and correct TLFs, edit checks and SAS programs to ensure quality
  • Assist in the development of programming documentation including specifications
  • Provide technical expertise and project solutions
  • Fulfil project responsibilities at the level of assisting the statistical programming Team Lead (TL)
  • Understand timelines and milestones and alert TL to potential slippage
  • Work independently, act as technical lead and plan from time to time when required
  • Our perfect candidate needs the following :

  • Knowledge of statistics, programming and clinical drug development process
  • Working knowledge of Base SAS, SAS / STAT and SAS Macro Language
  • 2 years working knowledge of the ADaM standards in clinical trials
  • 2 years working knowledge of TLFs in clinical trials
  • Working knowledge of the SDTM structure
  • Master's Degree in Computer science or related field and 1 years relevant experience Or Bachelor's Degree Computer science or related field and 3 years relevant experience Or equivalent combination of education, training and experience
  • Already possess the right to work in the recruiting country (we cannot offer visas)
  • Ability to estimate programming scope of work and implement programming specifications
  • Excellent accuracy, attention to detail, organizational, interpersonal and communication skills
  • Ability to establish working relationships with co-workers, managers and clients
  • You’re an especially great match if you have :

  • In-depth knowledge of applicable clinical research regulatory requirements would be an advantage; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • LI-PC5

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